7721
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Methyl-CpG binding protein 2 |
AUTSX3, MRX16, MRX79, MRXS13, MRXSL, PPMX, RS, RTS, RTT |
Angelman syndrome, Anxiety disorder, Attention deficit hyperactivity disorder, Rett syndrome, Autism, Autism, x-linked, Bruxism, Bulbar palsy, Hepatocellular carcinoma, Central apnea, Chromosome xq28 duplication syndrome, Congenital neurologic anomalies, Craniofacial abnormalities, Cyclin-dependent kinase-like 5 deficiency, Developmental disability, Developmental regression, Digestive system disease, Partial epilepsy, Epilepsy, Developmental and epileptic encephalopathy, Global developmental delay, Gross motor development delay, Hearing impairment, Hyperalgesia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Learning disorders, Systemic lupus erythematosus, Micrognathism, Neurodevelopmental disorder, X-linked intellectual disability, Psychiatric disorders, Pulmonary fibrosis, Rheumatoid arthritis, Schizophrenia, Seizures, Neonatal encephalopathy, Sick sinus syndromeView all (23 more) |
7722
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Mitochondrial trans-2-enoyl-CoA reductase |
CGI-63, DYTOABG, ETR1, FASN2B, NRBF1, OPA16 |
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7723
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|
Mediator complex subunit 1 |
CRSP1, CRSP200, DRIP205, DRIP230, PBP, PPARBP, PPARGBP, RB18A, TRAP220, TRIP2 |
|
7724
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|
|
Mediator complex subunit 10 |
L6, NUT2, TRG20 |
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7725
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|
|
Mediator complex subunit 11 |
HSPC296, NDDRSB |
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7726
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|
|
Mediator complex subunit 12 |
ARC240, CAGH45, FGS1, HDKR, HOPA, Kto, MED12S, OHDOX, OKS, OPA1, TNRC11, TRAP230 |
Imperforate anus, Blepharophimosis syndrome, Blepharophimosis-intellectual disability syndrome, Breast neoplasms, Dilated cardiomyopathy, Cholestasis-pigmentary retinopathy-cleft palate syndrome, Major depressive disorder, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Non-organic psychosis, Prostatic neoplasms, Psychotic disorders, Schizophrenia, Simpson-golabi-behmel syndrome, Depression, X-linked intellectual disabilityView all (4 more) |
7727
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|
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Mediator complex subunit 12L |
NIZIDS, NOPAR, TNRC11L, TRALP, TRALPUSH |
Alzheimer disease, Nonsyndromic intellectual disability, Platelet-type bleeding disorder, Developmental disability, Digestive system disease, Diverticular disease, Insomnia, Intellectual developmental disorder, Irritable bowel syndrome, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Parkinson disease, Thrombocytopenia |
7728
|
|
|
Mediator complex subunit 13 |
ARC250, DRIP250, HSPC221, MRD61, THRAP1, TRAP240 |
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7729
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|
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Mediator complex subunit 13L |
MRFACD, PROSIT240, THRAP2, TRAP240L |
Autism, Breast cancer, Cardiac anomalies - developmental delay - facial dysmorphism syndrome, Central nervous system cancer, Congenital camptodactyly, Congenital heart disease, Corneal astigmatism, Crohn disease, Melanoma, Developmental delay, Developmental delay with facial dysmorphism syndrome, Discordant ventriculoarterial connection, Glioblastoma, Glioma, Global developmental delay, Inflammatory bowel disease, Intellectual developmental disorder, Intellectual disability, Neurodevelopmental disorder, Scoliosis, Strabismus, Tetralogy of fallot, Transposition of the great arteries, Vesicoureteral refluxView all (9 more) |
7730
|
|
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Mediator complex subunit 14 |
CRSP150, CRSP2, CSRP, CXorf4, DRIP150, EXLM1, RGR1, TRAP170 |
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